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MPS I stands for Mucopolysacchardosis type I. It is an inherited genetic disorder caused by a deficiency in an enzyme called alpha-L-iduronidase (IDUA)
Learn MoreDisease management for MPS I can include supportive and symptom-based management and disease-specific management. Early intervention is important.
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Living with MPS I is a lifelong journey for patients and their families. Over a period of years, MPS I may present a range of challenges and experiences that may vary from individual to individual.
Learn MoreThe MPS I Registry program, sponsored and administered by Sanofi Genzyme, is a worldwide database that has been tracking health-related information for people with MPS I since 2003, allowing doctors and health care professionals to understand the disorder. Ask your doctor for more information.
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In this section, you’ll find valuable resources that can provide additional support and options for further learning:
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